JP6144698B2 - Hiv複製の阻害剤としての縮合三環式化合物 - Google Patents
Hiv複製の阻害剤としての縮合三環式化合物 Download PDFInfo
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- JP6144698B2 JP6144698B2 JP2014547651A JP2014547651A JP6144698B2 JP 6144698 B2 JP6144698 B2 JP 6144698B2 JP 2014547651 A JP2014547651 A JP 2014547651A JP 2014547651 A JP2014547651 A JP 2014547651A JP 6144698 B2 JP6144698 B2 JP 6144698B2
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- XFCRCZYNRQHVDP-UHFFFAOYSA-N CC1(C)OB(c2ccc(CO)nc2)OC1(C)C Chemical compound CC1(C)OB(c2ccc(CO)nc2)OC1(C)C XFCRCZYNRQHVDP-UHFFFAOYSA-N 0.000 description 1
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- ZRNKUTOZXNSMHD-UHFFFAOYSA-N CCOc(nc12)ccc1[o]c(C(c(nc1)ccc1OC)=N1)c2NC1=O Chemical compound CCOc(nc12)ccc1[o]c(C(c(nc1)ccc1OC)=N1)c2NC1=O ZRNKUTOZXNSMHD-UHFFFAOYSA-N 0.000 description 1
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- WGNSXDQCODKFJS-STQMWFEESA-N CC[C@@H](C1)OCC[C@@H]1N(c(c1n2)c(C(c3c[n](C)nc3)=N3)[o]c1ccc2Cl)C3=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c(c1n2)c(C(c3c[n](C)nc3)=N3)[o]c1ccc2Cl)C3=O WGNSXDQCODKFJS-STQMWFEESA-N 0.000 description 1
- KYFIOKGDIPRPOW-WBUKYKKZSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(/C(/C)=C/N(C)N=C)=N2)[o]c3c1cc(-c1c[n](C)nc1)c(Cl)c3)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(/C(/C)=C/N(C)N=C)=N2)[o]c3c1cc(-c1c[n](C)nc1)c(Cl)c3)C2=O KYFIOKGDIPRPOW-WBUKYKKZSA-N 0.000 description 1
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- UEGAVSKVQXLELD-GJZGRUSLSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-[n]4ncnc4)nc13)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-[n]4ncnc4)nc13)C2=O UEGAVSKVQXLELD-GJZGRUSLSA-N 0.000 description 1
- UDCSVXIJKDIPHF-QMMMGPOBSA-N CC[C@@H]1OCCC2(CC2)C1 Chemical compound CC[C@@H]1OCCC2(CC2)C1 UDCSVXIJKDIPHF-QMMMGPOBSA-N 0.000 description 1
- XIQCSACWJUJZCL-WPRPVWTQSA-N C[C@@H](C1)[C@]11OCCC2(CC2)C1 Chemical compound C[C@@H](C1)[C@]11OCCC2(CC2)C1 XIQCSACWJUJZCL-WPRPVWTQSA-N 0.000 description 1
- XIQCSACWJUJZCL-HNHGDDPOSA-N C[C@H](C1)C11OCCC2(CC2)C1 Chemical compound C[C@H](C1)C11OCCC2(CC2)C1 XIQCSACWJUJZCL-HNHGDDPOSA-N 0.000 description 1
- KIOKOKYISCAPLD-HALDLXJZSA-N C[C@H](C1)O[C@@H](C)C[C@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-c4c[n](C)nc4)nc13)C2=O Chemical compound C[C@H](C1)O[C@@H](C)C[C@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-c4c[n](C)nc4)nc13)C2=O KIOKOKYISCAPLD-HALDLXJZSA-N 0.000 description 1
- IXJSDKIJPVSPKF-UHFFFAOYSA-N C[n]1ncc(Br)c1 Chemical compound C[n]1ncc(Br)c1 IXJSDKIJPVSPKF-UHFFFAOYSA-N 0.000 description 1
- NBJYPQMOABEZIF-UHFFFAOYSA-N Cc(c(-c1c[n](C)nc1)c1)cc2c1c(NC(N=C1c3c[n](C)nc3)=O)c1[o]2 Chemical compound Cc(c(-c1c[n](C)nc1)c1)cc2c1c(NC(N=C1c3c[n](C)nc3)=O)c1[o]2 NBJYPQMOABEZIF-UHFFFAOYSA-N 0.000 description 1
- MYUQKYGWKHTRPG-UHFFFAOYSA-N Fc(nc1)ccc1Br Chemical compound Fc(nc1)ccc1Br MYUQKYGWKHTRPG-UHFFFAOYSA-N 0.000 description 1
- ZYLBLRYYAAIKMO-YGPZHTELSA-N N=CCC(C1)[C@@H]1NCC1CC1 Chemical compound N=CCC(C1)[C@@H]1NCC1CC1 ZYLBLRYYAAIKMO-YGPZHTELSA-N 0.000 description 1
- XJBHWDKRZXYEDL-UHFFFAOYSA-N OCCC1OCCCC1 Chemical compound OCCC1OCCCC1 XJBHWDKRZXYEDL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
- C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161578008P | 2011-12-20 | 2011-12-20 | |
| US61/578,008 | 2011-12-20 | ||
| PCT/CA2012/050909 WO2013091096A1 (en) | 2011-12-20 | 2012-12-19 | Condensed triclyclic compounds as inhibitors of hiv replication |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015500843A JP2015500843A (ja) | 2015-01-08 |
| JP2015500843A5 JP2015500843A5 (enExample) | 2016-02-18 |
| JP6144698B2 true JP6144698B2 (ja) | 2017-06-07 |
Family
ID=48667578
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014547651A Active JP6144698B2 (ja) | 2011-12-20 | 2012-12-19 | Hiv複製の阻害剤としての縮合三環式化合物 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US9399645B2 (enExample) |
| EP (1) | EP2794613B1 (enExample) |
| JP (1) | JP6144698B2 (enExample) |
| WO (1) | WO2013091096A1 (enExample) |
Families Citing this family (109)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2840095A1 (en) | 2011-07-06 | 2013-01-10 | Gilead Sciences, Inc. | Compounds for the treatment of hiv |
| WO2015089327A1 (en) | 2013-12-11 | 2015-06-18 | Biogen Idec Ma Inc. | Biaryl compounds useful for the treatment of human diseases in oncology, neurology and immunology |
| TW201613916A (en) | 2014-06-03 | 2016-04-16 | Gilead Sciences Inc | TANK-binding kinase inhibitor compounds |
| TW201613936A (en) | 2014-06-20 | 2016-04-16 | Gilead Sciences Inc | Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide |
| NO2717902T3 (enExample) | 2014-06-20 | 2018-06-23 | ||
| US20160067255A1 (en) | 2014-09-04 | 2016-03-10 | Gilead Sciences, Inc. | Methods of treating or preventing hiv in patients using a combination of tenofovir alafenamide and dolutegravir |
| TWI695003B (zh) | 2014-12-23 | 2020-06-01 | 美商基利科學股份有限公司 | 多環胺甲醯基吡啶酮化合物及其醫藥用途 |
| TWI770552B (zh) | 2014-12-24 | 2022-07-11 | 美商基利科學股份有限公司 | 喹唑啉化合物 |
| SG11201705184PA (en) | 2014-12-24 | 2017-07-28 | Gilead Sciences Inc | Isoquinoline compounds for the treatment of hiv |
| CA2972014C (en) | 2014-12-24 | 2019-09-24 | Gilead Sciences, Inc. | Fused pyrimidine compounds for the treatment of hiv |
| SG11201606876RA (en) | 2015-03-04 | 2016-10-28 | Gilead Sciences Inc | Toll like receptor modulator compounds |
| CA2980362C (en) | 2015-04-02 | 2020-02-25 | Gilead Sciences, Inc. | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
| MA42684A (fr) | 2015-08-26 | 2018-07-04 | Gilead Sciences Inc | Modulateurs deutérés du récepteur toll |
| CA2999516A1 (en) | 2015-09-30 | 2017-04-06 | Gilead Sciences, Inc. | Compounds and combinations for the treatment of hiv |
| JP6732915B2 (ja) | 2015-12-15 | 2020-07-29 | ギリアード サイエンシーズ, インコーポレイテッド | ヒト免疫不全ウイルス中和抗体 |
| WO2017172368A1 (en) | 2016-03-31 | 2017-10-05 | Oncternal Therapeutics, Inc. | Indoline analogs and uses thereof |
| LT3347352T (lt) | 2016-08-19 | 2019-08-12 | Gilead Sciences, Inc. | Terapiniai junginiai, naudotini živ viruso infekcijos profilaktikai arba terapiniam gydymui |
| WO2018042331A1 (en) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinations and uses and treatments thereof |
| WO2018042332A1 (en) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinations and uses and treatments thereof |
| SI3507276T1 (sl) | 2016-09-02 | 2022-01-31 | Gilead Sciences, Inc. | Spojine modulatorja toličnih receptorjev |
| WO2018045150A1 (en) | 2016-09-02 | 2018-03-08 | Gilead Sciences, Inc. | 4,6-diamino-pyrido[3,2-d]pyrimidine derivaties as toll like receptor modulators |
| WO2018051250A1 (en) | 2016-09-14 | 2018-03-22 | Viiv Healthcare Company | Combination comprising tenofovir alafenamide, bictegravir and 3tc |
| EP3519409B1 (en) | 2016-09-28 | 2024-09-18 | Gilead Sciences, Inc. | Benzothiazol-6-yl acetic acid derivatives and their use for treating hiv infection |
| EP3532478B1 (en) | 2016-10-27 | 2021-05-26 | Gilead Sciences, Inc. | Crystalline form of darunavir free base |
| CN106632019B (zh) * | 2016-12-28 | 2019-05-28 | 太原理工大学 | 一种多取代吡啶的制备方法 |
| TWI714820B (zh) | 2017-01-31 | 2021-01-01 | 美商基利科學股份有限公司 | 替諾福韋艾拉酚胺(tenofovir alafenamide)之晶型 |
| UY37592A (es) | 2017-02-06 | 2018-08-31 | Gilead Sciences Inc | Compuestos inhibidores del vih |
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| US7642277B2 (en) | 2002-12-04 | 2010-01-05 | Boehringer Ingelheim International Gmbh | Non-nucleoside reverse transcriptase inhibitors |
| JP2009525310A (ja) | 2006-02-03 | 2009-07-09 | テイボテク・フアーマシユーチカルズ・リミテツド | 突然変異したhivを処置する方法 |
| BRPI1014821A2 (pt) * | 2009-04-09 | 2016-04-05 | Boehringer Ingelheim Int | "inibidores de replicação de hiv" |
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